Related Experiment Video
Updated: Aug 4, 2026

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Naïve Adolescents at High Risk for Psychosis
Published on: November 21, 2013
Sodium valproate and tardive dyskinesia
Sodium valproate did not improve tardive dyskinesia symptoms in schizophrenic patients. A one-month trial showed no significant changes in involuntary movements associated with neuroleptic medication.
Area of Science:
- Neuroscience
- Psychiatry
- Pharmacology
Background:
- Tardive dyskinesia (TD) is a movement disorder associated with long-term antipsychotic use.
- Existing treatments for TD have limited efficacy and significant side effects.
- Sodium valproate is an anticonvulsant with potential mood-stabilizing and anti-movement properties.
Purpose of the Study:
- To evaluate the efficacy of sodium valproate in treating tardive dyskinesia in patients with schizophrenia.
- To determine if adjunctive sodium valproate can reduce the severity of TD symptoms.
Main Methods:
- A one-month, open-label study involving 25 schizophrenic patients diagnosed with tardive dyskinesia.
- Patients received a daily dose of 600 mg of sodium valproate in addition to their existing neuroleptic medication.
- Symptom severity was assessed by a panel of nine raters who reviewed video recordings taken before and after the treatment period.
Main Results:
- No significant improvement in tardive dyskinesia signs was observed after one month of treatment.
- The panel of raters did not detect any reduction in the severity of involuntary movements.
- Adjunctive sodium valproate at 600 mg/day did not demonstrate therapeutic benefit for TD in this patient group.
Conclusions:
- Sodium valproate, at a dose of 600 mg daily, is not effective in treating tardive dyskinesia in schizophrenic patients.
- Further research with different dosages or in different patient populations may be warranted.
- This study suggests that sodium valproate is not a viable treatment option for tardive dyskinesia.
Related Concept Videos
Antipsychotic Drugs: Typical and Atypical Agents
Antiepileptic Drugs: Sodium Channel Blockers
Sodium channel blockers modulate ion channels, particularly voltage-gated sodium channels. They block only sodium ion movement.
Among the most commonly prescribed antiepileptic drugs are...
Antiepileptic Drugs: GABAergic Pathway Potentiators
The key GABA pathway potentiators used in epilepsy management are as follows.
Benzodiazepines are a well-known class of drugs used for their...
Antiepileptic Drugs: Calcium Channel Blockers
Calcium channel blockers exert their antiepileptic effects by targeting T-type calcium channels, which are integral to transmitting nerve signals in the central nervous system. These channels allow the passage of calcium ions, which are vital for neuronal communication. By inhibiting T-type calcium channels, calcium channel blockers effectively reduce the release of neurotransmitters and...
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...

